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NDC 51206-0201-02 UltraCare 200 mg/mL Details

UltraCare 200 mg/mL

UltraCare is a DENTAL GEL in the HUMAN OTC DRUG category. It is labeled and distributed by Ultradent Products, Inc.. The primary component is BENZOCAINE.

Product Information

NDC	51206-0201
Product ID	51206-201_ef1abc86-26ba-48a2-b40f-a2f4a5291545
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	UltraCare
Proprietary Name Suffix	Oral Anesthetic Bubble Gum
Non-Proprietary Name	Benzocaine
Product Type	HUMAN OTC DRUG
Dosage Form	GEL
Route	DENTAL
Active Ingredient Strength	200
Active Ingredient Units	mg/mL
Substance Name	BENZOCAINE
Labeler Name	Ultradent Products, Inc.
Pharmaceutical Class	Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part356
Listing Certified Through	n/a

Package

Package Images

NDC 51206-0201-02 (51206020102)

Pricing Information	N/A
NDC Package Code	51206-201-02
Billing NDC	51206020102
Package	1 SYRINGE, PLASTIC in 1 BOX (51206-201-02) / 30 mL in 1 SYRINGE, PLASTIC
Marketing Start Date	1986-06-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL fd4a668a-28eb-4abc-b944-d17da3397510 Details

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Benzocaine 20% w/v

Purpose

Oral Anesthetic

Uses

For the temporary relief of occasional minor irritation and pain associated with

minor dental procedures
sore mouth and throat
minor injury of the gums
canker sores
minor irritation of the mouth or gums caused by dentures or orthodontic appliances.

Warnings

Methemoglobinemia warning

Use of this product may cause methemoglobinemia, a serious condition that must be treated promptly because it reduces the amount of oxygen carried in blood. This can occur even if you have used this product before. Stop use and seek immediate medical attention if you or a child in your care develops:

pale, gray, or blue colored skin (cyanosis)
headache
rapid heart rate
shortness of breath
dizziness or lightheadedness
fatigue or lack of energy.

For external use only

Allergy alert

Do not use if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics, PABA compounds, or sunscreen. If a skin reaction occurs, stop use and seek medical help right away.

Sore throat warning

if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. If sore mouth symptoms do not improve in 7 days, or if irritation, pain, or redness persist or worsens, see your dentist or doctor promptly.

Do not use

if taking sulfonamides
for teething
in children under 2 years of age

When using this product

avoid contact with eyes.

Keep out of reach of children. in case of overdose, get medical help or contact a Poison Control Center right away. Do not exceed recommended dosage.

Directions

Adults and children 2 years of age and older	Apply a thin film to affected area. Allow to remain in place at least 1 minute and then spit out. Use up to 4 times daily or as directed by your dentist or doctor.
Children between 2 and 12 years of age	Should be supervised in the use of this product.
Children under 2 years of age	Do not use.

Other information

Phenylketonurics: Contains Phenylalanine 3 mg per gram
Do not use if tamper-evident seal is broken
Store at room temperature

Inactive ingredients

aspartame, ethyl alcohol, FD&C red no. 40, glycerin, natural and artificial flavors, polyethylene glycol, sodium saccharin, titanium dioxide

Questions or comments?

800.552.5512

SPL UNCLASSIFIED SECTION

Manufactured by Ultradent Products, Inc.

505 West Ultradent Drive (10200 South), South Jordan, UT 84095

MEDICATION GUIDE

Ultracare®

ORAL ANESTHETIC GEL

Description:

Ultracare is a 20% w/v (17.9%) benzocaine oral anesthetic gel preparation in a water-soluble glycol base. Ultracare is designed for rapid onset (10-30 seconds). Anesthesia usually lasts 8-10 minutes. Ultracare is NOT for injection.

Uses:

For the temporary relief of occasional minor irritation and pain, associated with:

Minor dental procedures
Sore mouth and throat
Minor injury of the gums
Canker sores
Minor irritation of the mouth or gums caused by dentures or orthodontic appliances

Warnings:

Methemoglobinemia warning:

pale, gray, or blue colored skin (cyanosis)
headache
rapid heart rate
shortness of breath
dizziness or lightheadedness
fatigue or lack of energy.

For external use only

Allergy alert:

Sore throat warning:

If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. If sore mouth symptoms do not improve in 7 days, or if irritation, pain, or redness persist or worsens, see your dentist or doctor promptly.

Procedure:

1. Preloaded 1.2ml syringes: a. Remove luer lock cap from syringe. b. Attach a Blue Micro® 20-gauge Tip or 5mm Micro Capillary Tip securely onto syringe. c. Slowly express gel to the target tissue. d. For anesthetizing periodontal pockets: i. Slowly apply a small amount to one quadrant at a time to the gingival margin or directly into the periodontal pockets and proceed with sub-gingival scaling.	Fig. 1 Hold plunger in palm of hand for optimum control. Fig. 2 Deliver Ultracare from the large, no-waste IndiSpense syringe to cotton applicator, cotton roll, etc., for placement.
2. IndiSpense® delivery: a. Remove cap from IndiSpense syringe. b. Express desired amount of anesthetic to cotton applicator (Fig. 2) or into a dappen dish. Use a clean applicator with each area application. Re-cap the IndiSpense syringe after each use. c. Using a dappen dish allows for re-application with the same applicator without the risk of cross-contamination. Re-cap the IndiSpense syringe after each use. 3. IndiSpense delivery to empty 1.2ml syringe: a. Attach a 1.2ml syringe to the end of IndiSpense by turning the luer lock of the 1.2ml syringe snugly onto male thread of Indispense syringe. b. With palm, press plunger of IndiSpense syringe gently while guiding the 1.2ml plunger outward to desired fill. c. RE-cap the IndiSpense syringe after each use. d. See instruction for 1.2ml syringe use.

Directions:

Adults and children 2 years of age and older:

Apply a thin film to affected area. Allow to remain in place at least 1 minute and then spit out. Use up to 4 times daily or as directed by your dentist or doctor.
Rinse and expectorate to clear the oral cavity of residual product.
Apply a thin film to injection site(s) allowing the gelled cotton applicator to remain in place at least 1 minute.
Rinse and suction the oral cavity and continue with administering local anesthetic or with dental procedure.

For anesthetizing periodontal pockets:

See instruction for 1.2ml use.

Children between 2 and 12 years of age:

Should be supervised in the use of this product

Children under 2 years of age:

Do not use

Warnings and Precautions:

1.: For Professional use only.
2.: For external use only.
3.: Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
4.: Ultracare is NOT for injection.
5.: Pregnancy and Lactation: Safety is not known in pregnancy/nursing women.
6.: Avoid contact with eyes.
7.: If applying intraorally from a syringe, verify flow on a gauze pad or mixing pad prior to applying. If resistance is met, replace tip and re-check.
8.: If an excessive amount of gel is swallowed, get medical help or contact a Poison Control Center immediately.
9.: Do not exceed maximum recommended dosage.
10.: Phenylketonurics: Contains Phenylalanine—3mg per gram
11.: See state or country guidelines for proper disposal of empty jar, syringes, applicator and tips.
12.: To avoid cross-contamination of the prefilled syringes, use a disposable syringe cover, re-cap, and wipe syringe with an intermediate disinfectant between uses. If these measures are not taken, the syringes should be considered single-use. Tips are disposable. To avoid cross-contamination, do not re-use tips.

For immediate reorder and/or complete descriptions of Ultradent's product line, refer to Ultradent's catalog or call Toll Free: 1-800-552-5512. Outside U.S. call (801) 572-4200.

All Ultradent syringes have an expiration date stamped on the side of the syringe consisting of one letter and three numbers. The letter is a lot number used for manufacturing purposes and the three numbers are the expiration date. The first two numbers are the month, and the third number is the last number of the year.

PRINCIPAL DISPLAY PANEL - 30 mL Syringe Label

Ultracare®

Oral Anesthetic Gel

Bubble Gum

REF/UP 357

ULTRADENT

PRODUCTS, INC.

1.01 FL OZ (30 mL) IndiSpense®

Made in USA | 33329.14 062518

PRINCIPAL DISPLAY PANEL - 30 mL Syringe Label

INGREDIENTS AND APPEARANCE

ULTRACARE ORAL ANESTHETIC BUBBLE GUM

benzocaine gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:51206-201
Route of Administration	DENTAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Benzocaine (UNII: U3RSY48JW5) (Benzocaine - UNII:U3RSY48JW5)	Benzocaine	200 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
Aspartame (UNII: Z0H242BBR1)
Alcohol (UNII: 3K9958V90M)
FD&C Red No. 40 (UNII: WZB9127XOA)
Glycerin (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
Saccharin Sodium (UNII: SB8ZUX40TY)
Titanium Dioxide (UNII: 15FIX9V2JP)

Product Characteristics
Color	PINK	Score
Shape		Size
Flavor	BUBBLE GUM	Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:51206-201-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/1986	06/18/2023
2	NDC:51206-201-02	1 in 1 BOX	06/01/1986	08/31/2024
2		30 mL in 1 SYRINGE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH NOT FINAL	part356	06/01/1986	08/31/2024

Labeler - Ultradent Products, Inc. (013369913)

Name	Address	ID/FEI	Business Operations
Establishment
Ultradent Products, Inc.		013369913	MANUFACTURE(51206-201) , ANALYSIS(51206-201) , LABEL(51206-201) , PACK(51206-201)

Revised: 4/2021

Document Id: ef1abc86-26ba-48a2-b40f-a2f4a5291545

Set id: fd4a668a-28eb-4abc-b944-d17da3397510

Version: 8

Effective Time: 20210401

Search by Drug Name or NDC

NDC 51206-0201-02 UltraCare 200 mg/mL Details

UltraCare 200 mg/mL

Product Information

Package

Package Images

NDC 51206-0201-02 (51206020102)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL fd4a668a-28eb-4abc-b944-d17da3397510 Details

SPL UNCLASSIFIED SECTION

Active ingredient

Purpose

Uses

Warnings

Methemoglobinemia warning

Allergy alert

Sore throat warning

Do not use

When using this product

Directions

Other information

Inactive ingredients

Questions or comments?

SPL UNCLASSIFIED SECTION

MEDICATION GUIDE

PRINCIPAL DISPLAY PANEL - 30 mL Syringe Label

INGREDIENTS AND APPEARANCE

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